Kojic Acid Effect on the Inhibitory Potency of Tyrosinase

الموضوعات :

Forogh Azami ¹ , Elham Tazikeh-Lemeski ² , Mehr-Ali Mahmood-Janlou ³

1 - Department of Biology, Gorgan Branch, Islamic Azad University, Gorgan, Iran
2 - Department of Chemistry, Gorgan Branch, Islamic Azad University, Gorgan, Iran
3 - Department of Biology, Gorgan Branch, Islamic Azad University, Gorgan, Iran

تاريخ الإرسال : 29 الأربعاء , رجب, 1438 تاريخ التأكيد : 20 الإثنين , صفر, 1440 تاريخ الإصدار : 29 الأربعاء , رجب, 1438

الکلمات المفتاحية: Molecular docking, Binding Energy, Kojic acid, Tyrosinase, Inhibition Constant,

ملخص المقالة :

In recent years, enzymatic activity of tyrosinase has been the focus of investigation due to its potential applications in medicine, agriculture and cosmetics. Tyrosinase, entitled polyphenol oxidase, is a key enzyme that catalyzes synthesis of melanin in plants, microorganisms and mammalian cells. Presence of some antioxidants can delay or inhibit the activity of this enzyme as well. In this survey, molecular docking calculation method using Autodock 4.0 software for prediction of binding energy of the protein with some antioxidant ligands was executed. The pose with the lowest energy of binding or inhibition constant was extracted at 298.15 K for kojic acid. Number of conformations in the cluster of rank was 13. The first and second boxes free energy and the inhibition constant were as follows: -5.60 kcalmol-1, 78.99 µM and -3.32 kcalmol-1, 3.66 µM, respectively. Since the first box presented a lower value of free energy, it was considered as the best mode of structure of kojic acid and the protein docking for further analysis. Thus, our present study could contribute to development and discernment of tyrosinase inhibitors in order to prevent hyper pigmentation.

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